Since the BAC libraries are build using partial HindIII digestion, a bias in the sampling of the genomic sequences is expected.
Indeed, the number of nucleotides damaged by mutagens in coding sequences is expected to be inversely proportional to the size of the non-coding DNA fraction.
Therefore, the generation of additional dinoflagellate Hsp90 sequences is expected to refine the stem group of athecate species observed here and contribute to future multi-gene analyses of dinoflagellate interrelationships.
Surface exposure of the interactive sequences is expected for the functional effects of αB crystallin on microtubule assembly which can only occur on the surface of dissociated subunits of αB crystallin or tubulin.
In addition, the coverage of the ribosomal reference databases, compared to the true distribution of all existing ribosomal sequences, is expected to be much better than the coverage of Genbank nr compared to all existing protein coding sequences.
Thus, one out of 10 single copy sequences is expected to be covered.
The availability of complete genome sequences is expected to dramatically deliver a high impact on biology.
Removal of these sequences is expected to create HBP/SLBP isoforms with different properties.
